A single-cell RNA-seq atlas of Schistosoma mansoni identifies a key regulator of blood feeding

被引:96
|
作者
Wendt, George [1 ]
Zhao, Lu [1 ]
Chen, Rui [1 ]
Liu, Chenxi [2 ]
O'Donoghue, Anthony J. [2 ]
Caffrey, Conor R. [2 ]
Reese, Michael L. [1 ,3 ]
Collins, James J., III [1 ]
机构
[1] UT Southwestern Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
[2] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, Ctr Discovery & Innovat Parasit Dis, 9500 Gilman Dr, La Jolla, CA 92093 USA
[3] UT Southwestern Med Ctr, Dept Biochem, Dallas, TX 75390 USA
基金
英国惠康基金; 美国国家科学基金会;
关键词
CATHEPSIN-B; EXPRESSION;
D O I
10.1126/science.abb7709
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Schistosomiasis is a neglected tropical disease that infects 240 million people. With no vaccines and only one drug available, new therapeutic targets are needed. The causative agents, schistosomes, are intravascular flatworm parasites that feed on blood and lay eggs, resulting in pathology. The function of the parasite's various tissues in successful parasitism are poorly understood, hindering identification of therapeutic targets. Using single-cell RNA sequencing (RNA-seq), we characterize 43,642 cells from the adult schistosome and identify 68 distinct cell populations, including specialized stem cells that maintain the parasite's blood-digesting gut. These stem cells express the gene hnf4, which is required for gut maintenance, blood feeding, and pathology in vivo. Together, these data provide molecular insights into the organ systems of this important pathogen and identify potential therapeutic targets.
引用
收藏
页码:1644 / +
页数:36
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